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The ERK MAP kinase pathway mediates induction of SGK (serum‐ and glucocorticoid‐inducible kinase) by growth factors
Author(s) -
Mizuno Hiroshi,
Nishida Eisuke
Publication year - 2001
Publication title -
genes to cells
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.912
H-Index - 115
eISSN - 1365-2443
pISSN - 1356-9597
DOI - 10.1046/j.1365-2443.2001.00418.x
Subject(s) - mapk/erk pathway , biology , cycloheximide , kinase , mitogen activated protein kinase , protein kinase b , signal transduction , mek inhibitor , microbiology and biotechnology , cancer research , protein biosynthesis
Background The ERK MAP kinase pathway plays a pivotal role in growth factor‐induced gene expression. However, genes whose expression is induced by the ERK pathway are not fully defined. Results We have identified SGK (serum‐ and glucocorticoid‐inducible kinase) as an ERK‐inducible gene by the subtractive screening of Raf‐inducible genes. SGK is known to be similar in primary structure to AKT/PKB, PKC and PKA. Treatment of quiescent NIH‐3T3 cells with FGF, PDGF or TPA, which induced the sustained activation of ERKs, resulted in the strong induction of SGK, whereas treatment with EGF, which induced the transient activation of ERKs, did not induce a strong expression of SGK. The induction of SGK was blocked by pre‐treatment with a specific MEK inhibitor U0126, and expression of constitutively active MEK was able to induce SGK. Treatment with cycloheximide or vanadate prolonged the increased expression of SGK by FGF, concomitant with a more prolonged activation of ERKs. Conclusion Growth factor‐induced activation of the ERK MAP kinase pathway is necessary and sufficient for the induction of SGK.